|
ENST00000646891.2:c.2140A>G
MANE Select
|
ENSP00000493543.1:p.Ile714Val
|
|
|
ENST00000288602.11:c.2260A>G
|
ENSP00000288602.7:p.Ile754Val
|
|
|
ENST00000479537.6:c.892A>G
|
|
|
|
ENST00000496384.7:c.2140A>G
|
ENSP00000419060.2:p.Ile714Val
|
|
|
ENST00000497784.2:c.*1590A>G
|
ENSP00000420119.2:n.*1590A>G
|
|
|
ENST00000642228.1:c.*1218A>G
|
ENSP00000493678.1:n.*1218A>G
|
|
|
ENST00000642875.1:n.1538A>G
|
|
|
|
ENST00000644120.1:n.2517+5054A>G
|
|
|
|
ENST00000644650.1:c.1439A>G
|
|
|
|
ENST00000644905.1:n.3022A>G
|
|
|
|
ENST00000644969.2:c.2260A>G
MANE Plus Clinical
|
ENSP00000496776.1:p.Ile754Val
|
|
|
ENST00000645443.1:n.1919A>G
|
|
|
|
ENST00000646730.1:c.*798A>G
|
ENSP00000494784.1:n.*798A>G
|
|
|
ENST00000646891.1:c.2140A>G
|
ENSP00000493543.1:p.Ile714Val
|
|
|
ENST00000647434.1:c.1017A>G
|
ENSP00000495132.1:n.1017A>G
|
|
|
ENST00000288602.10:c.2140A>G
|
ENSP00000288602.6:p.Ile714Val
|
|
|
ENST00000479537.5:c.506A>G
|
ENSP00000418033.1:n.506A>G
|
|
|
ENST00000496384.6:c.963A>G
|
|
|
|
ENST00000497784.1:c.2175A>G
|
ENSP00000420119.1:n.2175A>G
|
|
|
NM_004333.4:c.2140A>G , LRG_299t1:c.2140A>G
|
NP_004324.2:p.Ile714Val
|
|
|
XM_005250045.1:c.2140A>G
|
XP_005250102.1:p.Ile714Val
|
|
|
XM_005250046.1:c.2127+5054A>G
|
XP_005250103.1:n.2127+5054A>G
|
|
|
XM_011516529.1:c.2127+5054A>G
|
XP_011514831.1:n.2127+5054A>G
|
|
|
XR_242190.1:n.2230A>G
|
|
|
|
XR_927520.1:n.2269A>G
|
|
|
|
XR_927521.1:n.2351A>G
|
|
|
|
XR_927522.1:n.1982A>G
|
|
|
|
XR_927523.1:n.2064A>G
|
|
|
|
NM_001354609.1:c.2140A>G
|
NP_001341538.1:p.Ile714Val
|
|
|
NM_004333.5:c.2140A>G
|
NP_004324.2:p.Ile714Val
|
|
|
NR_148928.1:n.3238A>G
|
|
|
|
XM_017012558.1:c.2260A>G
|
XP_016868047.1:p.Ile754Val
|
|
|
XM_017012559.1:c.2247+5054A>G
|
XP_016868048.1:n.2247+5054A>G
|
|
|
XR_001744857.1:n.2350A>G
|
|
|
|
XR_001744858.1:n.2102A>G
|
|
|
|
NM_001354609.2:c.2140A>G
|
NP_001341538.1:p.Ile714Val
|
|
|
NM_001374244.1:c.2260A>G
|
NP_001361173.1:p.Ile754Val
|
|
|
NM_001374258.1:c.2260A>G
MANE Plus Clinical
|
NP_001361187.1:p.Ile754Val
|
|
|
NM_004333.6:c.2140A>G
MANE Select
|
NP_004324.2:p.Ile714Val
|
|
|
NM_001378467.1:c.2149A>G
|
NP_001365396.1:p.Ile717Val
|
|
|
NM_001378468.1:c.2127+5054A>G
|
NP_001365397.1:n.2127+5054A>G
|
|
|
NM_001378469.1:c.2074A>G
|
NP_001365398.1:p.Ile692Val
|
|
|
NM_001378470.1:c.2038A>G
|
NP_001365399.1:p.Ile680Val
|
|
|
NM_001378471.1:c.2029A>G
|
NP_001365400.1:p.Ile677Val
|
|
|
NM_001378472.1:c.1984A>G
|
NP_001365401.1:p.Ile662Val
|
|
|
NM_001378473.1:c.1984A>G
|
NP_001365402.1:p.Ile662Val
|
|
|
NM_001378474.1:c.2127+5054A>G
|
NP_001365403.1:n.2127+5054A>G
|
|
|
NM_001378475.1:c.1876A>G
|
NP_001365404.1:p.Ile626Val
|
|
